Canonical Allele Identifier: CA2429774919

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53248132C= , CM000685.2:g.53248132C=	GRCh38
NC_000023.10:g.53277314C= , CM000685.1:g.53277314C=	GRCh37
NC_000023.9:g.53294039C=	NCBI36
NG_021296.1:g.78209G=
NG_021296.2:g.78219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2723G=	ENSP00000516672.1:p.Arg908=
ENST00000638521.1:c.516G=
ENST00000638869.1:c.25G=
ENST00000640694.1:c.2564G=	ENSP00000492403.1:p.Arg855=
ENST00000642864.1:c.2564G= MANE Select	ENSP00000495726.1:p.Arg855=
ENST00000674510.1:c.2564G=	ENSP00000502054.1:p.Arg855=
ENST00000674761.1:n.315G=
ENST00000675719.1:c.2534G=	ENSP00000501927.1:p.Arg845=
ENST00000375365.2:c.1949G=	ENSP00000364514.2:p.Arg650=
ENST00000396435.7:c.2564G=	ENSP00000379712.3:p.Arg855=
NM_001111125.2:c.2564G=	NP_001104595.1:p.Arg855=
NM_015075.1:c.1949G=	NP_055890.1:p.Arg650=
XM_006724579.2:c.2660G=	XP_006724642.1:p.Arg887=
XM_006724580.2:c.1949G=	XP_006724643.1:p.Arg650=
XM_006724581.2:c.2660G=	XP_006724644.1:p.Arg887=
XM_006724582.2:c.2660G=	XP_006724645.1:p.Arg887=
XM_006724583.2:c.2660G=	XP_006724646.1:p.Arg887=
XM_006724584.2:c.2660G=	XP_006724647.1:p.Arg887=
XM_011530772.1:c.1886G=	XP_011529074.1:p.Arg629=
XM_011530773.1:c.1853G=	XP_011529075.1:p.Arg618=
XM_011530774.1:c.2660G=	XP_011529076.1:p.Arg887=
XM_011530775.1:c.2660G=	XP_011529077.1:p.Arg887=
XM_011530776.1:c.2660G=	XP_011529078.1:p.Arg887=
XM_011530777.1:c.2660G=	XP_011529079.1:p.Arg887=
XR_938365.1:n.2887G=
XM_006724579.3:c.2660G=	XP_006724642.1:p.Arg887=
XM_006724580.3:c.1949G=	XP_006724643.1:p.Arg650=
XM_006724581.4:c.2660G=	XP_006724644.1:p.Arg887=
XM_006724582.4:c.2660G=	XP_006724645.1:p.Arg887=
XM_006724583.4:c.2660G=	XP_006724646.1:p.Arg887=
XM_006724584.3:c.2660G=	XP_006724647.1:p.Arg887=
XM_011530773.2:c.1853G=	XP_011529075.1:p.Arg618=
XM_011530774.3:c.2660G=	XP_011529076.1:p.Arg887=
XM_011530776.2:c.2660G=	XP_011529078.1:p.Arg887=
XM_011530777.2:c.2660G=	XP_011529079.1:p.Arg887=
XM_017029359.2:c.2534G=	XP_016884848.1:p.Arg845=
XM_017029360.1:c.2066G=	XP_016884849.1:p.Arg689=
XR_938365.2:n.2881G=
NM_001111125.3:c.2564G= MANE Select	NP_001104595.1:p.Arg855=
NM_015075.2:c.1949G=	NP_055890.1:p.Arg650=